Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Koichi, Kamei"'
Autor:
Eri Ohashi, MD, Itaru Hayakawa, MD, Yoshiyuki Tsutsumi, MD, Koichi Kamei, MD,PHD, Kentaro Ide, MD, Yuichi Abe, MD,PHD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 10, Pp 3475-3480 (2022)
Central-variant posterior reversible encephalopathy syndrome is an atypical subtype of posterior reversible encephalopathy syndrome that occurs during rapid fluctuations in blood pressure, leading to cerebrovascular autoregulatory failure and endothe
Externí odkaz:
https://doaj.org/article/7fbf99304c5d496899a1fe6232822d30
Autor:
Kentaro Nishi, Masao Ogura, Naotaka Tamai, Naofumi Gima, Kentaro Ide, Goro Koinuma, Koichi Kamei, Shuichi Ito
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract Background Rapidly progressive (RP) interstitial lung disease (ILD) is a life-threatening complication of juvenile dermatomyositis (JDM); however, it is generally refractory to treatment; to the best of our knowledge, no evidence-based treat
Externí odkaz:
https://doaj.org/article/e62fc85a1b4047dcb9de1e866f9dd3ba
Autor:
Teizaburo Mori, Akihiro Fujino, Masataka Takahashi, Ryoya Furugane, Tamotsu Kobayashi, Motohiro Kano, Akihiro Yoneda, Yutaka Kanamori, Ryutaro Suzuki, Kentaro Nishi, Koichi Kamei, Masayuki Kitamura
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-7 (2021)
Abstract Background Pleuroperitoneal communication (PPC) is an uncommon, but potentially life-threatening complication of peritoneal dialysis (PD). If a fistula does not close with conservative treatment, surgical repair is required. However, approxi
Externí odkaz:
https://doaj.org/article/7da883ad915845cb87cd14b168f3055f
Autor:
Ryoya Furugane, Tamotsu Kobayashi, Naoki Hashizume, Teizaburo Mori, Eiichiro Watanabe, Motohiro Kano, Masataka Takahashi, Miki Murakoshi, Mai Sato, Koichi Kamei, Akihiro Fujino, Akihiro Yoneda, Yutaka Kanamori
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 76, Iss , Pp 102131- (2022)
Outflow obstruction of a catheter for peritoneal dialysis (PD) is one of the most common complications in patients who are undergoing PD for renal failure. Although the cause of catheter obstruction is variable, a choked catheter caused by a fallopia
Externí odkaz:
https://doaj.org/article/b1cb8257184c4082aa80cea97b6b46fb
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Thrombotic microangiopathy (TMA) is a histopathological entity associated with microangiopathic hemolytic anemia, thrombocytopenia, and end-organ ischemic damage. Although TMA is caused by various diseases, there have been few rep
Externí odkaz:
https://doaj.org/article/e945d5124a5a4ce18d61ff8dce0baaac
Autor:
Sho Ishiwa, Koichi Kamei, Kanako Tanase-Nakao, Shinsuke Shibata, Kunihiro Matsunami, Ichiro Takeuchi, Mai Sato, Kenji Ishikura, Satoshi Narumi
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background MIRAGE syndrome is a recently discovered rare genetic disease characterized by myelodysplasia (M), infection (I), growth restriction (R), adrenal hypoplasia (A), genital phenotypes (G), and enteropathy (E), caused by a gain-of-fun
Externí odkaz:
https://doaj.org/article/33bedf3d887a45e5af2b33bc0d95a0a9
Autor:
Georgia Malakasioti, Daniela Iancu, Anastasiia Milovanova, Alexey Tsygin, Tomoko Horinouchi, China Nagano, Kandai Nozu, Koichi Kamei, Shuichiro Fujinaga, Kazumoto Iijima, Rajiv Sinha, Biswanath Basu, William Morello, Giovanni Montini, Aoife Waters, Olivia Boyer, Zeynep Yürük Yıldırım, Sibel Yel, İsmail Dursun, Hugh J. McCarthy, Marina Vivarelli, Larisa Prikhodina, Martine T.P. Besouw, Eugene Yu-hin Chan, Wenyan Huang, Markus J. Kemper, Sebastian Loos, Chanel Prestidge, William Wong, Galia Zlatanova, Rasmus Ehren, Lutz T. Weber, Hassib Chehade, Nakysa Hooman, Marcin Tkaczyk, Małgorzata Stańczyk, Michael Miligkos, Kjell Tullus
Publikováno v:
Kidney International, 103(5), 962-972. ELSEVIER SCIENCE INC
While 44-83% of children with steroid-resistant nephrotic syndrome (SRNS) without a proven genetic cause respond to treatment with a calcineurin inhibitor (CNI), current guidelines recommend against the use of immunosuppression in monogenic SRNS. Thi
Autor:
Kentaro Nishi, Masao Ogura, Naotaka Tamai, Masafumi Gima, Kentaro Ide, Goro Koinuma, Koichi Kamei, Shuichi Ito
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/75b3bd2637924659b1da1ab8170ed3d7
Autor:
China Nagano, Mayumi Sako, Koichi Kamei, Kenji Ishikura, Hidefumi Nakamura, Koichi Nakanishi, Takashi Omori, Kandai Nozu, Kazumoto Iijima
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-10 (2019)
Abstract Background Eighty percent of children with idiopathic nephrotic syndrome respond well to steroid therapy, but up to 50% of patients with steroid-sensitive nephrotic syndrome exhibit frequently relapsing (FRNS) or steroid-dependent nephrotic
Externí odkaz:
https://doaj.org/article/b61729eaf0484f3290f3150c0bc4d81b
Autor:
Ken Saida, Masao Ogura, Yuji Kano, Shingo Ishimori, Takahisa Yoshikawa, Hiroko Nagata, Mai Sato, Koichi Kamei, Kenji Ishikura
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-4 (2018)
Abstract Background Bordetella pertussis infection is a known trigger of atypical hemolytic uremic syndrome (HUS). For patients suspected of having atypical HUS, prompt plasma exchange/infusion (PE/PI) or eculizumab (ECZ) treatment is recommended. Ca
Externí odkaz:
https://doaj.org/article/e17056703b114332a6e3665e731e3504